Metoclopramide Hydrochloride
- Product NDC
- 71335-0522
- 11-digit product format
- 713350522
- Labeler code
- 71335
- Product ID
- 71335-0522_7cd0f1be-b5cd-4ee8-827b-0048a0ecc7b9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoclopramide Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA071250
- Marketing category
- ANDA
- Marketing start
- 2011-08-22
- Marketing end
- 0000-00-00
- Substance
- METOCLOPRAMIDE HYDROCHLORIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Dopamine D2 Antagonists [MoA],Dopamine-2 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-0522-1 | 71335052201 | 30 TABLET in 1 BOTTLE (71335-0522-1) | 30 tablet | 2017-05-01 | 0000-00-00 | No | No | Current |
| 71335-0522-2 | 71335052202 | 90 TABLET in 1 BOTTLE (71335-0522-2) | 90 tablet | 2017-05-01 | 0000-00-00 | No | No | Current |
| 71335-0522-3 | 71335052203 | 60 TABLET in 1 BOTTLE (71335-0522-3) | 60 tablet | 2017-05-01 | 0000-00-00 | No | No | Current |
| 71335-0522-4 | 71335052204 | 10 TABLET in 1 BOTTLE (71335-0522-4) | 10 tablet | 2017-05-01 | 0000-00-00 | No | No | Current |
| 71335-0522-5 | 71335052205 | 20 TABLET in 1 BOTTLE (71335-0522-5) | 20 tablet | 2017-05-01 | 0000-00-00 | No | No | Current |
| 71335-0522-6 | 71335052206 | 100 TABLET in 1 BOTTLE (71335-0522-6) | 100 tablet | 2017-05-01 | 0000-00-00 | No | No | Current |